# FDA device recall: REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following instruments:   - B1018-280 MicroScan 

> recall · VERIFIED · 2026-06-26

Firm: Beckman Coulter Inc. · Class II · Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."

- Company: Beckman Coulter Inc.
- Sector: diagnostics
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.